@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_head
{
this:
np:hasAssertion
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_assertion
;
np:hasProvenance
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_provenance
;
np:hasPublicationInfo
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_assertion
a
np:Assertion
.
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_provenance
a
np:Provenance
.
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_assertion
{
miriam-gene:4041
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGNe180cd3127bd5e1a17b9191550811b74
sio:SIO_000628
miriam-gene:4041
,
lld:C0029456
;
a
sio:SIO_001121
.
}
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_provenance
{
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_assertion
dcterms:description
"[In this article, we present the extensive genetic and functional data indicating that the LRP5 gene and the Wnt signalling pathway are key players in bone formation and the risk of osteoporosis, and that LRP5 signalling is essential for normal morphology, developmental processes and bone health.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15760771
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP472363.RAFK3S0ZJhXOvz2lkLddexdp-UIXzQ6OjYmupaaVHkhNo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}